NDC 68016-128 Diaperrashointment

NDC Product Code 68016-128

NDC 68016-128-20

Package Description: 113 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Diaperrashointment with NDC 68016-128 is a product labeled by Pharmacy Value Alliance, Llc. The generic name of Diaperrashointment is . The product's dosage form is and is administered via form.

Labeler Name: Pharmacy Value Alliance, Llc

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Pharmacy Value Alliance, Llc
Labeler Code: 68016
Start Marketing Date: 08-22-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: E What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Diaperrashointment Product Label Images

Diaperrashointment Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Zinc Oxide 40%

Purpose

Skin Protectant

Uses

  • Helps treat and prevent diaper rashProtects chafed skin due to diaper rash and helps protect skin from wetness

Keep Out Of The Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Warnings

  • For External Use OnlyWhen using this productAvoid contact with eyes

Directions

  • Change wet and soiled diapers promptlyCleanse the diaper area and allow to dryApply ointment liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

Stop Use And Ask A Doctor If

  • Condition worsensSymptoms last more than 7 days or clear up and occur again with a few days

Other Information:

  • Store at controlled room temperature 20° - 25°C (68° - 77°F)

Inactive Ingredients

BHA, Cod liver oil (high in vitamin A and D), Frangrance, Lanolin, Mineral Oil, Methylparaben, Petrolatum, Purified water, Talc, Tartrazine yellow #4 (FD and C yellow #4)

Helps Treat And Prevent Diaper Rash. Protects Skin. Relieves Chafing. Promotes Healing

Distributed by:Pharmacy Value Alliance, LLC.407 East Lancaster Avenue, Wayne, PA. 19087 USAwww.emersongroup.com

* Please review the disclaimer below.